FGG - fibrinogen gamma chain Gene

Homo sapiens

Gene ID: 2266 | Gene type: protein coding

About FGG

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:154,604,136-154,612,656 (from NCBI)

This gene has 12 transcripts (splice variants), 208 orthologues, 25 paralogues and is associated with 6 phenotypes. Restricted expression toward liver (RPKM 3614.5).

Summary

The protein encoded by this gene is the gamma component of fibrinogen, a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains. Following vascular injury, fibrinogen is cleaved by Thrombin to form fibrin which is the most abundant component of blood clots. In addition, various cleavage products of fibrinogen and fibrin regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Mutations in this gene lead to several disorders, including dysfibrinogenemia, hypofibrinogenemia and thrombophilia. Alternative splicing results in transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]

FGG Products(2)

mRNA	Protein	Name
NM_000509.6	NP_000500.2	fibrinogen gamma chain isoform gamma-A precursor
NM_021870.3	NP_068656.2	fibrinogen gamma chain isoform gamma-B precursor

FGG Protein Structure

Fib_alpha

Fibrinogen_C

0
100
200
300
400
453 a.a.

Protein Preferred Names

Protein Names

fibrinogen gamma chain

fibrinogen, gamma polypeptide

Recombinant FGG Proteins

Cat. No.	Product Name	Accession	Purity
HY-P75772	FGG/Fibrinogen gamma chain Protein, Human (P.pastoris)	P02679 (V169-L453)	≥95%

Related Diseases

Diseases

Alias

Afibrinogenemia, Congenital

Congenital Afibrinogenemia	Afibrinogenemia
Factor I Deficiency	Familial Afibrinogenemia
Hypofibrinogenemia, Congenital	Fibrinogen Deficiency
Afibrinogenemia Congenital	CAFBN
Congenital Hypofibrinogenemia	Hypofibrinogenemia
Complement Factor I Deficiency

Dysfibrinogenemia, Congenital

Dysfibrinogenemia	Hypodysfibrinogenemia
Familial Dysfibrinogenemia	Familial Hypodysfibrinogenemia
Hypodysfibrinogenemia, Congenital	Dysfibrinogenemia, Familial
Congenital Dysfibrinogenemia	DYSFIBRIN

Hypofibrinogenemia, Familial

Familial Hypofibrinogenemia

Fibrinogen Deficiency, Congenital

Congenital Fibrinogen Deficiency

Thrombosis

Thrombosis Of Blood Vessel

Thrombophilia

Hypercoagulability State

Thrombocytopenia

Low Platelet Count	Low Platelets
Decreased Platelets	Platelet Dysfunction Nos

Femoral Vein Thrombophlebitis

Phlebitis And Thrombophlebitis Of Femoral Vein	Thrombophlebitis Of The Femoral Vein
Thrombophlebitis Of Deep Femoral Vein

Alopecia-Mental Retardation Syndrome 1

APMR1	Alopecia-Intellectual Disability Syndrome 1
Amr Syndrome	Alopecia-Intellectual Disability Syndrome
Amr Syndrome 1	Alopecia With Severe Intellectual Deficit
Apmr	Alopecia Intellectual Disbility Syndrome 1
Perniola-Krajewska-Carnevale Syndrome	Alopecia - Intellectual Disability Syndrome
Alopecia With Mental Retardation Syndrome 1	Perniola Krajewska Carnevale Syndrome

Gingival Recession

Localized Gingival Recession	Gingival Recession, Localized
Minimal Gingival Recession	Moderate Gingival Recession
Severe Gingival Recession	Gingival Recession, Minimal
Gingival Recession, Severe	Atrophy Of Gums
Gum Atrophy	Gingival Atrophy

Intermediate Malignant Teratoma

Malignant Teratoma, Intermediate

Intermediate Immature Teratoma

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04925	FGG Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	FGG	VGNC	VGNC:54208
Rattus norvegicus	FGG	RGD	RGD:2613
Mus musculus	FGG	MGD	MGI:95526
Felis catus	FGG	VGNC	VGNC:62261
Macaca mulatta	FGG	VGNC	VGNC:72656
Bos taurus	FGG	VGNC	VGNC:28990
Others	FGG	NCBI